The Vollrath Company LLC

FDA Device Registration & Listing · Kiel, WI, US · Registration 2183714

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
2183714
FEI Number
2183714
Entity Name
The Vollrath Company LLC
City/State/Country
Kiel, WI, US
Establishment Address
502 Hwy. 67, Kiel, WI 53042, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
The Vollrath Co., LLC (Owner Number: 2183714)
Owner / Operator Contact Address
502 Hwy. 67, --, Kiel, WI 53042, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FNP Urinal General Hospital Class 1 880.6730 2009-06-05
IKW Utensil, Homemaking Physical Medicine Class 1 890.5050 2023-02-28
FNY Basin, Emesis General Hospital Class 1 880.6730 1992-07-02
FOB Bedpan General Hospital Class 1 880.6730 1992-07-02

Official Correspondent

Kristian Heiberger

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

The Vollrath Co., LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
2182202 VOLLRATH COMPANY LLC, THE Sheboygan, WI, US

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2183714. Last updated year: 2026. Please use registration number 2183714 when referencing this establishment in official correspondence.
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